A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1 ; volume:9 ; number:1 ; day:24 ; month:1 ; year:2019 ; pages:1-7 ; date:12.2019
Scientific reports ; 9, Heft 1 (24.1.2019), 1-7, 12.2019
- Creator
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Grønskov, Karen
Jespersgaard, Cathrine
Bruun, Gitte Hoffmann
Harris, Pernille
Brøndum-Nielsen, Karen
Andresen, Brage S.
Rosenberg, Thomas
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-018-37272-5
- URN
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urn:nbn:de:101:1-2019022222543589551738
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Grønskov, Karen
- Jespersgaard, Cathrine
- Bruun, Gitte Hoffmann
- Harris, Pernille
- Brøndum-Nielsen, Karen
- Andresen, Brage S.
- Rosenberg, Thomas
- SpringerLink (Online service)
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